Artificial intelligence and neurodegeneration: state of the art and explainability.

IF 3.8 Q2 OPHTHALMOLOGY
Emanuele Crincoli, Maria Cristina Savastano, Alfonso Savastano, Matteo Mario Carlà, Federico Giannuzzi, Fiammetta Catania, Raphael Kilian, Clara Rizzo, Stanislao Rizzo
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引用次数: 0

Abstract

Background: Alzheimer disease (AD) and Parkinson disease (PD) are an increasing healthcare concern and growing cause of disability in our century. The advent of the artificial intelligence (AI) era and the early changes in retina and optic nerve morphology detected in neurodegenerative diseases by recent literature opened the way to the perspective of a AI-based diagnosis for both conditions.

Main body: In AD a generalized decrease in macular Ganglion Cells-Inner Plexiform Layer (GC-IPL) and retinal nerve fiber layer (RNFL) and peripapillary RNFL thickness has been documented. Moreover, clinical AD is characterized by a lower choroidal thickness and higher choroidal vascularity index. AI can be predicted with around 80% accuracy based on small fundus vessels characteristics. Similarly, AI based on Optical Coherence Tomography (OCT) images showed very good performance in detecting AD, especially based on total macular volume (TVM) and GCL thickness. A combination of OCT and color fundus photographs (CFP) imaging reached 85% accuracy in detecting MCI. In PD typical retinal anomalies include a generalized thinning of the peripapillary RNFL with a degeneration pattern similar to the one of mitochondrial optic neuropathies, foveal pit widening, generalized retinal and retinal pigmented epithelium thinning and outer plexiform layer thickening. AI CFP-based detection of PD showed only 65% accuracy due to a low specificity, while multimodal imaging-based AI was the best approach, reaching a 100% sensitivity and 85% specificity.

Conclusion: In consideration of the overall very good performance, AD and PD are likely to benefit from the support of retinal-imaging based AI for early diagnosis. To optimize the performance, especially in terms of specificity, the use of multimodal imaging and possible integration with meta-data has been demonstrated to be the best technique, especially for PD diagnosis. However, training and testing on a larger sample size and longitudinal evaluation of the chosen models will be needed before application on general population. So far, explainability of the proposed models seems robust and coherent with the corresponding central nervous system damage.

人工智能和神经退行性变:最新进展和可解释性。
背景:阿尔茨海默病(AD)和帕金森病(PD)是本世纪日益受到关注的健康问题和日益增长的致残原因。人工智能(AI)时代的到来,以及最近文献中发现的神经退行性疾病中视网膜和视神经形态的早期变化,为这两种疾病的人工智能诊断开辟了道路。正文:在AD中,黄斑神经节细胞-内丛状层(GC-IPL)和视网膜神经纤维层(RNFL)和乳头周围RNFL厚度普遍减少。此外,临床AD的特点是脉络膜厚度较低,脉络膜血管指数较高。基于眼底小血管的特征,人工智能的预测准确率在80%左右。同样,基于光学相干断层扫描(OCT)图像的人工智能在检测AD方面表现出非常好的性能,特别是基于黄斑总体积(TVM)和GCL厚度。结合OCT和彩色眼底照片(CFP)成像检测MCI的准确率达到85%。PD患者典型的视网膜异常包括乳头周围RNFL广泛性变薄,其变性模式与线粒体视神经病变相似,中央凹增宽,视网膜和视网膜色素上皮广泛性变薄,外网状层增厚。基于AI cfp的PD检测由于特异性较低,准确率仅为65%,而基于多模态成像的AI是最佳方法,达到100%的灵敏度和85%的特异性。结论:考虑到AD和PD的整体表现非常好,基于视网膜成像的人工智能支持AD和PD的早期诊断可能会受益。为了优化性能,特别是在特异性方面,使用多模态成像和可能的整合元数据已被证明是最好的技术,特别是对于PD诊断。然而,在应用于一般人群之前,需要在更大的样本量上进行训练和测试,并对所选模型进行纵向评估。到目前为止,所提出的模型的可解释性似乎与相应的中枢神经系统损伤是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
4.30%
发文量
81
审稿时长
19 weeks
期刊介绍: International Journal of Retina and Vitreous focuses on the ophthalmic subspecialty of vitreoretinal disorders. The journal presents original articles on new approaches to diagnosis, outcomes of clinical trials, innovations in pharmacological therapy and surgical techniques, as well as basic science advances that impact clinical practice. Topical areas include, but are not limited to: -Imaging of the retina, choroid and vitreous -Innovations in optical coherence tomography (OCT) -Small-gauge vitrectomy, retinal detachment, chromovitrectomy -Electroretinography (ERG), microperimetry, other functional tests -Intraocular tumors -Retinal pharmacotherapy & drug delivery -Diabetic retinopathy & other vascular diseases -Age-related macular degeneration (AMD) & other macular entities
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